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cone-rod
NextBio Summary
General Info
Curated Studies
Most Correlated Studies
Mouse Phenotypes - Unspecified hereditary retinal dystrophies
OMIM - Retinal dystrophy
OMIM - Spondylometaphyseal dysplasia
OMIM - Progressive cone-rod dystrophy
OMIM - Cone-rod synaptic disorder
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Literature
Most Relevant Literature
Identification of a novel RPGR mutation associated with X-linked cone-rod dystrophy in a Chinese fam…
Novel TTLL5 Variants Associated with Cone-Rod Dystrophy and Early-Onset Severe Retinal Dystrophy.
The genetics of rod-cone dystrophy in Arab countries: a systematic review.
Clinical characteristics, imaging findings, and genetic results of a patient with CEP290-related con…
Homozygous mutation in ABCA4 associated with cone rod dystrophy in a patient with Turner syndrome.
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Clinical Trials
Most Relevant Clinical Trials
Rod and Cone Mediated Function in Retinal Disease
Interferon Gamma-1b Administered Topically for Macular Edema/Intraretinal Schisis Cysts in Rod-Cone …
Rod Sensitivity in Age-related Macular Degeneration (AMD) and Retinitis Pigmentosa (RP)
Study of New Mutations in Cone Disorders
Qualification for Cone-Optogenetics
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